Canonical Allele Identifier: CA398625452

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18057505G>A (hg19) ; chr17:g.18154191G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154191G>A , CM000679.2:g.18154191G>A	GRCh38
NC_000017.10:g.18057505G>A , CM000679.1:g.18057505G>A	GRCh37
NC_000017.9:g.17998230G>A	NCBI36
NG_011634.1:g.50486G>A
NG_011634.2:g.50486G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644795.1:c.-61+1G>A	ENSP00000495720.1:n.-61+1G>A
ENST00000646782.1:n.303+1G>A
ENST00000647165.2:c.8148+1G>A MANE Select	ENSP00000495481.1:n.8148+1G>A
ENST00000651214.1:n.294+1G>A
ENST00000205890.9:c.8148+1G>A	ENSP00000205890.5:n.8148+1G>A
ENST00000418233.7:c.-61+1G>A	ENSP00000408800.3:n.-61+1G>A
ENST00000445289.6:n.137+1G>A
ENST00000536811.5:n.137+1G>A
ENST00000585180.1:c.-61+1G>A	ENSP00000464462.1:n.-61+1G>A
ENST00000615845.4:c.8148+1G>A	ENSP00000481642.1:n.8148+1G>A
NM_016239.3:c.8148+1G>A	NP_057323.3:n.8148+1G>A
XM_011523921.1:c.8142+1G>A	XP_011522223.1:n.8142+1G>A
XM_017024714.2:c.8088+1G>A	XP_016880203.1:n.8088+1G>A
XM_017024715.2:c.8151+1G>A	XP_016880204.1:n.8151+1G>A
XR_001752809.1:n.246C>T
XR_001752810.1:n.246C>T
NM_016239.4:c.8148+1G>A MANE Select	NP_057323.3:n.8148+1G>A